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Sponsored by: |
Centre Hospitalier Universitaire Dijon |
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Information provided by: | Centre Hospitalier Universitaire Dijon |
ClinicalTrials.gov Identifier: | NCT00629044 |
The aim of this study is to assess the implicitement of the cholesterol 24 S hydroxylase gene and the 24 S hydroxycholesterol in glaucoma and in age related macular degeneration.
Condition | Intervention |
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Glaucoma |
Biological: Assessing the blood level of cholesterol 24 S Hydroxylase Biological: Assessing the blood level of cholesterol 24 S hydroxylase Biological: assessing the blood level of cholesterol 24 S hydroxylase |
Study Type: | Interventional |
Study Design: | Screening, Non-Randomized, Open Label, Dose Comparison, Parallel Assignment |
Official Title: | Etude du Polymorphysme génétique de la cholestérol 24S Hydroxylase et Des Teneurs en 24S hydroxycholestérol Chez Des Patients Atteints de Glaucome ou de dégénérescence Maculaire liée à l'âge. |
Estimated Enrollment: | 320 |
Study Start Date: | November 2007 |
Estimated Primary Completion Date: | November 2009 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
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G: Active Comparator |
Biological: Assessing the blood level of cholesterol 24 S Hydroxylase
Comparison of venous blood level of Cholesterol 24 S hydroxylase and 24 hydroxycholesterol in patients with Glaucoma and AMD and in healthy subjects.
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AMD: Active Comparator |
Biological: Assessing the blood level of cholesterol 24 S hydroxylase
Comparison of venous blood level of cholesterol 24 S hydroxylase and 24 hydroxycholesterol in patients with Glaucoma, AMD end in healthy subjects
|
Healthy subjects: Active Comparator |
Biological: assessing the blood level of cholesterol 24 S hydroxylase
Comparison of venous blood level of cholesterol 24 S hydroxylase and 24 hydroxycholesterol in patients with glaucoma, AMD and in healthy subjects
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Ages Eligible for Study: | 40 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
Contact: Frédéric Nicot, CRA | 33 3 80293756 | frederic.nicot@chu-dijon.fr |
France, Burgundy | |
Ophthalmology Unit CHU Dijon | Recruiting |
Dijon, Burgundy, France, 21000 | |
Contact: Frédéric Nicot, CRA 33 3 80293756 frederic.nicot@chu-dijon.fr | |
Principal Investigator: Catherine Creuzot-Garcher, MD, PhD |
Principal Investigator: | Catherine Creuzot-Gracher, MD, PhD | CHU Dijon |
Responsible Party: | CHU Dijon ( Professor Catherine Creuzot-Garcher ) |
Study ID Numbers: | PHRC IR 2006 |
Study First Received: | February 25, 2008 |
Last Updated: | February 25, 2008 |
ClinicalTrials.gov Identifier: | NCT00629044 |
Health Authority: | France: Afssaps - French Health Products Safety Agency |
Glaucoma Eye Diseases Hypertension Ocular Hypertension |